JP2011521903A5 - - Google Patents
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- JP2011521903A5 JP2011521903A5 JP2011506435A JP2011506435A JP2011521903A5 JP 2011521903 A5 JP2011521903 A5 JP 2011521903A5 JP 2011506435 A JP2011506435 A JP 2011506435A JP 2011506435 A JP2011506435 A JP 2011506435A JP 2011521903 A5 JP2011521903 A5 JP 2011521903A5
- Authority
- JP
- Japan
- Prior art keywords
- pharmaceutically acceptable
- alkyl
- virus
- acceptable salt
- compound
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims description 49
- 150000003839 salts Chemical class 0.000 claims description 28
- 239000011780 sodium chloride Substances 0.000 claims description 28
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 24
- 230000002401 inhibitory effect Effects 0.000 claims description 18
- 239000003112 inhibitor Substances 0.000 claims description 16
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 14
- 229910052736 halogen Inorganic materials 0.000 claims description 14
- 150000002367 halogens Chemical class 0.000 claims description 14
- 239000003814 drug Substances 0.000 claims description 13
- 125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 12
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 12
- 241000700605 Viruses Species 0.000 claims description 10
- 229910052717 sulfur Inorganic materials 0.000 claims description 10
- 208000001756 Virus Disease Diseases 0.000 claims description 9
- 206010047461 Viral infection Diseases 0.000 claims description 8
- 125000005884 carbocyclylalkyl group Chemical group 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 125000003107 substituted aryl group Chemical group 0.000 claims description 8
- 230000017613 viral reproduction Effects 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 125000001072 heteroaryl group Chemical group 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 6
- 125000004426 substituted alkynyl group Chemical group 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 5
- 241000710780 Bovine viral diarrhea virus 1 Species 0.000 claims description 4
- 241000725619 Dengue virus Species 0.000 claims description 4
- 241000710781 Flaviviridae Species 0.000 claims description 4
- 101700014732 GCS1 Proteins 0.000 claims description 4
- 241000711549 Hepacivirus C Species 0.000 claims description 4
- 102000014150 Interferons Human genes 0.000 claims description 4
- 108010050904 Interferons Proteins 0.000 claims description 4
- 241000710842 Japanese encephalitis virus Species 0.000 claims description 4
- 241000710912 Kunjin virus Species 0.000 claims description 4
- 241000124008 Mammalia Species 0.000 claims description 4
- 241000710908 Murray Valley encephalitis virus Species 0.000 claims description 4
- 241000725177 Omsk hemorrhagic fever virus Species 0.000 claims description 4
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical class N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 claims description 4
- 241000710888 St. Louis encephalitis virus Species 0.000 claims description 4
- 241000710771 Tick-borne encephalitis virus Species 0.000 claims description 4
- 241000710886 West Nile virus Species 0.000 claims description 4
- 241000710772 Yellow fever virus Species 0.000 claims description 4
- 241000907316 Zika virus Species 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 239000000134 cyclophilin inhibitor Substances 0.000 claims description 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 4
- 239000002777 nucleoside Substances 0.000 claims description 4
- 150000003833 nucleoside derivatives Chemical class 0.000 claims description 4
- 239000000137 peptide hydrolase inhibitor Substances 0.000 claims description 4
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 4
- 229940051021 yellow-fever virus Drugs 0.000 claims description 4
- 229940042399 direct acting antivirals Protease inhibitors Drugs 0.000 claims description 3
- 229940079593 drugs Drugs 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims description 2
- 208000005176 Hepatitis C Diseases 0.000 claims description 2
- 229940047124 Interferons Drugs 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000000304 alkynyl group Chemical group 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 125000002837 carbocyclic group Chemical group 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 125000004122 cyclic group Chemical group 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims description 2
- 229940079322 interferon Drugs 0.000 claims description 2
- 229910052740 iodine Inorganic materials 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 239000000203 mixture Substances 0.000 claims 10
- -1 ethynyl compound Chemical class 0.000 claims 1
- 108010012057 RNA Replicase Proteins 0.000 description 2
- 150000007523 nucleic acids Chemical class 0.000 description 2
- 108020004707 nucleic acids Proteins 0.000 description 2
- FWKQNCXZGNBPFD-UHFFFAOYSA-N 1,4-dimethyl-7-(1-methylethyl)azulene Chemical compound CC(C)C1=CC=C(C)C2=CC=C(C)C2=C1 FWKQNCXZGNBPFD-UHFFFAOYSA-N 0.000 description 1
- 208000004576 Flaviviridae Infections Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 230000001413 cellular Effects 0.000 description 1
- 230000003612 virological Effects 0.000 description 1
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US4726308P | 2008-04-23 | 2008-04-23 | |
US61/047,263 | 2008-04-23 | ||
US13944908P | 2008-12-19 | 2008-12-19 | |
US61/139,449 | 2008-12-19 | ||
PCT/US2009/041447 WO2009132135A1 (en) | 2008-04-23 | 2009-04-22 | 1' -substituted carba-nucleoside analogs for antiviral treatment |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2013218129A Division JP2014040471A (ja) | 2008-04-23 | 2013-10-21 | 抗ウイルス処置のための1’−置換カルバ−ヌクレオシドアナログ |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2011521903A JP2011521903A (ja) | 2011-07-28 |
JP2011521903A5 true JP2011521903A5 (ru) | 2013-04-04 |
JP5425187B2 JP5425187B2 (ja) | 2014-02-26 |
Family
ID=40887058
Family Applications (4)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011506435A Active JP5425187B2 (ja) | 2008-04-23 | 2009-04-22 | 抗ウイルス処置のための1’−置換カルバ−ヌクレオシドアナログ |
JP2011506429A Active JP5425186B2 (ja) | 2008-04-23 | 2009-04-22 | 抗ウイルス処置のためのカルバ−ヌクレオシドアナログ |
JP2013218139A Withdrawn JP2014012739A (ja) | 2008-04-23 | 2013-10-21 | 抗ウイルス処置のためのカルバ−ヌクレオシドアナログ |
JP2013218129A Withdrawn JP2014040471A (ja) | 2008-04-23 | 2013-10-21 | 抗ウイルス処置のための1’−置換カルバ−ヌクレオシドアナログ |
Family Applications After (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2011506429A Active JP5425186B2 (ja) | 2008-04-23 | 2009-04-22 | 抗ウイルス処置のためのカルバ−ヌクレオシドアナログ |
JP2013218139A Withdrawn JP2014012739A (ja) | 2008-04-23 | 2013-10-21 | 抗ウイルス処置のためのカルバ−ヌクレオシドアナログ |
JP2013218129A Withdrawn JP2014040471A (ja) | 2008-04-23 | 2013-10-21 | 抗ウイルス処置のための1’−置換カルバ−ヌクレオシドアナログ |
Country Status (32)
Country | Link |
---|---|
US (5) | US8008264B2 (ru) |
EP (3) | EP2937350B9 (ru) |
JP (4) | JP5425187B2 (ru) |
KR (3) | KR101645742B1 (ru) |
CN (3) | CN104262345B (ru) |
AP (2) | AP3076A (ru) |
AR (1) | AR071395A1 (ru) |
AU (2) | AU2009240630B2 (ru) |
BR (2) | BRPI0910455B8 (ru) |
CA (2) | CA2722084C (ru) |
CO (2) | CO6321235A2 (ru) |
CY (4) | CY1113647T1 (ru) |
DK (3) | DK2268642T3 (ru) |
EA (2) | EA019883B1 (ru) |
EC (2) | ECSP10010609A (ru) |
ES (3) | ES2398684T3 (ru) |
HK (3) | HK1152709A1 (ru) |
HR (3) | HRP20130048T1 (ru) |
HU (3) | HUE038946T2 (ru) |
IL (2) | IL208515A (ru) |
LT (2) | LT2937350T (ru) |
ME (1) | ME03089B (ru) |
MX (2) | MX2010011659A (ru) |
NO (1) | NO2937350T3 (ru) |
NZ (2) | NZ588400A (ru) |
PL (3) | PL2268642T3 (ru) |
PT (3) | PT2268642E (ru) |
RS (2) | RS54008B1 (ru) |
SI (3) | SI2280973T1 (ru) |
TW (2) | TW201334784A (ru) |
WO (2) | WO2009132135A1 (ru) |
ZA (2) | ZA201007713B (ru) |
Families Citing this family (161)
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MY164523A (en) | 2000-05-23 | 2017-12-29 | Univ Degli Studi Cagliari | Methods and compositions for treating hepatitis c virus |
EA200601591A1 (ru) | 2000-05-26 | 2007-02-27 | Айденикс (Кайман) Лимитед | Применение рибонуклеозидных соединений для лечения флавивирусных и пестивирусных инфекций |
EP1576138B1 (en) | 2002-11-15 | 2017-02-01 | Idenix Pharmaceuticals LLC. | 2'-methyl nucleosides in combination with interferon and flaviviridae mutation |
WO2009132135A1 (en) | 2008-04-23 | 2009-10-29 | Gilead Sciences, Inc. | 1' -substituted carba-nucleoside analogs for antiviral treatment |
US8173621B2 (en) | 2008-06-11 | 2012-05-08 | Gilead Pharmasset Llc | Nucleoside cyclicphosphates |
EP2313102A2 (en) | 2008-07-03 | 2011-04-27 | Biota Scientific Management | Bycyclic nucleosides and nucleotides as therapeutic agents |
EP2364314B1 (en) | 2008-12-09 | 2014-03-12 | Gilead Sciences, Inc. | Modulators of toll-like receptors |
BRPI0922508A8 (pt) | 2008-12-23 | 2016-01-19 | Pharmasset Inc | Análogos de nucleosídeo |
CA2748057C (en) | 2008-12-23 | 2018-07-03 | Pharmasset, Inc. | Nucleoside phosphoramidates |
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US8618076B2 (en) | 2009-05-20 | 2013-12-31 | Gilead Pharmasset Llc | Nucleoside phosphoramidates |
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